# FDA recall D-0892-2018

> **Qualgen, LLC** · Class III · drug recall initiated 2018-06-08.

## Product

ESTRADIOL 20mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-020-01

## Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0892-2018
- **Recalling firm:** Qualgen, LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-06-08
- **Report date:** 2018-07-11
- **Termination date:** 2020-11-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Edmond, OK, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0892-2018

## Citation

> AI Analytics. FDA recall D-0892-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0892-2018. Source: US FDA. Licensed CC0.

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